A Comprehensive Assessment of Altered Embodiment in Individuals With Spinal Cord Injury

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorSwiss Paraplegic Research, Nottwil

About this trial

Spinal cord injury (SCI) occurs when trauma or other factors damage the spinal cord, disrupting the flow of sensory information from the body to the brain. This interruption can interfere with embodiment-the body awareness and physical sensations processed by the brain-sometimes leading to a phenomenon called disembodiment.

For people with SCI, disembodiment may appear as unusual body sensations, like feeling that a limb is in a different position than it actually is. Such changes in body awareness can impact daily life, mental health, and rehabilitation outcomes.

Despite its importance, the study of embodiment in SCI remains limited. This project aims to explore how SCI alters embodiment, focusing on its specific characteristics, the effects on daily life, and the underlying brain activity as measured by functional magnetic resonance imaging (fMRI). Both people with and without SCI will participate.

Procedure: Participants will complete a single examination lasting 2 to 2.5 hours, including approximately 55 minutes in the MRI scanner (with preparation and follow-up).

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age between 18 and 60

Normal or corrected-to-normal visual acuity

German or Italian native speaker

Diagnosis of traumatic spinal cord injury

Disqualifiers

Pregnancy or breastfeeding

Diagnosis of other psychiatric or neurological disorders (e.g. epilepsy, tumor in the central nervous system)

Confirmed diagnosis of alcohol and/or drug abuse with active consumption within the last 6 months

Confirmed diagnosis of traumatic brain injury, intended as visible changes in the brain diagnosed by a radiologist

Trial population

Individuals with spinal cord injury and healthy controls.

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • Behavioral assessment

    Behavioral

    A comprehensive behavioral assessment of embodiment and its effect on daily living, taking into account pain, interoception, emotions and anxiety, sleep quality, life satsfaction and cognition.

  • Functional Magnetic Resonance Imaging (fMRI)

    Behavioral

    Neural mechanisms of embodiments will be explored with MRI sequences including structural MRI, resting-state and task-based fMRI of the head. The task will be a modified version of the rubber hand illusion, previously used to asess embodiment. Participants will be required to lay in the MRI with their legs bended upright and a screen placed at the level of their hips, which will show a pair of legs. The participant's leg will be stroked with a paintbrush while the image on the screen will be showing the virtual legs being stroked. Participants will be required to report how strongly they perceive the virtual legs as their own, as a measure of embodiment.

Treatment groups

80 Participants
are divided into 4 treatment groups
Group A: Individuals with SCI - Behavioral assessment1 intervention
Group B: Individuals with SCI - Behavioral assessment and fMRI2 interventions
Group C: Healthy controls - Behavioral assessment1 intervention
Group D: Healthy controls - Behavioral assessment and fMRI2 interventions

Trial outcomes

Primary outcomes

1

Score on the Body Feelings and Illusions questionnaire (BoFI)

A questionnaires that assess different dimensions of embodiment and disembodiment.

Time frame
Baseline

Secondary outcomes

1

Brain activity

Brain activity defined as changes in oxygen levels in the blood during the execution of the embodiment task, and at rest.

Time frame
Baseline
2

Strenght of the embodiment illusion

Strenght of the embodiment illusion during the fMRI procedures, measured through a Likert scale.

Time frame
Baseline
3

Qualitative assessment of embodiment

Qualitative assessment of the experience of embodiment by means of a semi-structured interview.

Time frame
Baseline
4

Score on the WHO Disability Assessment Scale (WHODAS-II)

A scale that assesses activity limitation and participation restriction in the daily life due to disability.

Time frame
Baseline

Other outcomes

Sponsors and contacts

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